We’re seeking a proactive and experienced Supplier Quality Manager to lead our supplier oversight program and ensure the integrity of materials and products sourced externally. In this fast-paced, regulated environment, you’ll play a critical role in maintaining compliance, driving continuous improvement, and building strong supplier partnerships.

Key Responsibilities:

Evaluate and qualify new suppliers, ensuring alignment with GMP, GDP, and company standards.
Conduct routine and ad-hoc audits to assess supplier quality systems and capabilities.
Develop, negotiate, and manage supplier quality agreements.
Lead investigations into nonconformances and implement effective CAPAs.
Assess supplier changes (e.g., processes, locations) for impact on product quality and compliance.
Maintain accurate documentation including audit reports, change assessments, and CAPA records.
Collaborate cross-functionally with procurement, engineering, and manufacturing teams.
Monitor regulatory changes and ensure supplier activities meet GMP, CFR, ICH, and QAA requirements.
Maintain a database of supplier regulatory statements to support internal and customer assessments.
Identify and close gaps in supplier management programs and processes.

Qualifications

Bachelor’s degree in a related field required; advanced degree preferred.
5–10 years of quality assurance experience in pharmaceutical, healthcare or life sciences industry.
Deep knowledge of packaging systems and quality system regulations (21 CFR Parts 111, 210, 211, 820, 4).
Strong understanding industry guidelines and global compliance standards.
Proficient in Microsoft Office Suite and quality management systems.
Exceptional communication skills—written, verbal, and interpersonal.
Ability to coach and influence others in a collaborative, compliance-driven environment.

Why Join Us?

At Nutra-Med, we’re committed to quality, innovation, and continuous improvement. You’ll be part of a dynamic team that values expertise, collaboration, and the pursuit of excellence. If you’re ready to make a meaningful impact in a high-speed, high-stakes environment—we’d love to meet you.

We are proud to be an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity or expression, national origin, age, disability, veteran status, or any other legally protected status. We are committed to fostering a diverse and inclusive workplace where everyone feels valued and empowered to thrive.

You should be proficient in:

Quality Inspection Experience
FDA Regulations
Pharmaceuticals
Quality Control Experience
Packaging Experience